Subtilis
- Product NDC
- 49693-2301
- 11-digit product format
- 496932301
- Labeler code
- 49693
- Product ID
- 49693-2301_1b295707-cae6-4a8d-9d90-da81a54e3ab7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Bacillus subtilis
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- USPharmaCo
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-12-15
- Marketing end
- 0000-00-00
- Substance
- BACILLUS SUBTILIS
- Active strength
- 6 [hp_X]/5mL
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 49693-2301-1 | Subtilis | 5 mL in 1 BOTTLE | LIQUID | 5 | | 1 |
| 49693-2301-1 | Subtilis | 1 in 1 BOX | LIQUID | 1 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 49693-2301 | SUBTILIS (BACILLUS SUBTILIS) LIQUID [USPHARMACO] | 1 | Legacy NDC, 2 package rows | 20091223_21dc6b8a-f8ec-4073-a8b0-77af0d58fb88.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 49693-2301-1 | 49693230101 | 5 mL in 1 BOTTLE | 5 ml | Historical |